Zobrazeno 1 - 10
of 1 079
pro vyhledávání: '"Yukio Ando"'
Autor:
Yukio Ando, Marcia Waddington-Cruz, Yoshiki Sekijima, Haruki Koike, Mitsuharu Ueda, Hiroaki Konishi, Tomonori Ishii, Teresa Coelho
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-17 (2023)
Abstract Hereditary transthyretin (ATTRv) amyloidosis is a rare and autosomal dominant disorder associated with mutations in the transthyretin gene. Patients present with diverse symptoms related to sensory, motor, and autonomic neuropathy, as well a
Externí odkaz:
https://doaj.org/article/b4211bad5c5b4a2f92847c0a1e464bdc
Autor:
Kenta Ouchi, Kaori Isono, Yuki Ohya, Nobuaki Shiraki, Masayoshi Tasaki, Yukihiro Inomata, Mitsuharu Ueda, Takumi Era, Shoen Kume, Yukio Ando, Hirofumi Jono
Publikováno v:
Heliyon, Vol 10, Iss 2, Pp e24590- (2024)
Hereditary transthyretin (TTR) amyloidosis (ATTRv amyloidosis) is autosomal dominant and caused by mutation of TTR gene. Heterozygous ATTR Tyr114Cys (p.Tyr134Cys) amyloidosis is a lethal disease with a life expectancy of about 10 years after onset of
Externí odkaz:
https://doaj.org/article/a449e521100b47aebc43f6901a9e738b
Autor:
Yoshitaka Murakami, Fan-Yan Wei, Yoshimi Kawamura, Haruki Horiguchi, Tsuyoshi Kadomatsu, Keishi Miyata, Kyoko Miura, Yuichi Oike, Yukio Ando, Mitsuharu Ueda, Kazuhito Tomizawa, Takeshi Chujo
Publikováno v:
Communications Biology, Vol 6, Iss 1, Pp 1-12 (2023)
A mitochondrial tRNA modification enzyme, NSUN3, is found to be essential for embryonic development in mice, with whole-body knockout causing embryonic lethality and heart-specific Nsun3 knockout leading to heart aberration in older mice.
Externí odkaz:
https://doaj.org/article/18bce67c3ad3458da80e542465626a4f
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-10 (2023)
Abstract In patients with Parkinson’s disease (PD), α-synuclein pathology is thought to spread to the brain via the dorsal motor nucleus of the vagus nerve. The link between the gut microbiome and PD has been explored in various studies. The appen
Externí odkaz:
https://doaj.org/article/c507336e1d1047cb9f0cee44a6ef9e68
Autor:
Hiroaki Matsushita, Yohei Misumi, Teruaki Masuda, Masamitsu Okada, Fumika Inoue, Mitsuharu Ueda, Yukio Ando
Publikováno v:
Pathophysiology, Vol 29, Iss 3, Pp 333-343 (2022)
Transthyretin (TTR), the precursor protein for amyloidogenic TTR (ATTR) amyloidosis, forms tetramers and escapes glomerular filtration by binding with thyroxine and retinol-binding protein. However, variant TTRs are unstable as tetramers, so monomeri
Externí odkaz:
https://doaj.org/article/8f422b7c2a454860933618791a358e08
Autor:
Makoto Yamakawa, Shunya Nakane, Eikichi Ihara, Nozomu Tawara, Hiroko Ikeda, Yoko Igarashi, Yoshihiro Komohara, Koutaro Takamatsu, Tokunori Ikeda, Yusuke Tomita, Shoichi Murai, Yukio Ando, Akihiro Mukaino, Yoshihiro Ogawa, Mitsuharu Ueda
Publikováno v:
Frontiers in Neuroscience, Vol 16 (2022)
We aimed to establish a novel murine model of autoimmune autonomic ganglionopathy (AAG), which represents autoimmune dysautonomia, associated with MHC class II to understand its pathomechanism and the pathogenicity of nicotinic acetylcholine receptor
Externí odkaz:
https://doaj.org/article/f1f43928e24645b693104dde8df6a9f7
Autor:
Akira Taniguchi, Akihiro Shindo, Ken-ichi Tabei, Osamu Onodera, Yukio Ando, Takao Urabe, Kazumi Kimura, Kazuo Kitagawa, Yoshihiro Miyamoto, Misa Takegami, Masafumi Ihara, Ikuko Mizuta, Toshiki Mizuno, Hidekazu Tomimoto
Publikováno v:
Frontiers in Aging Neuroscience, Vol 14 (2022)
ObjectivesPatients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) show various clinical symptoms, including migraine, recurrent stroke, and cognitive impairment. We investigated the associati
Externí odkaz:
https://doaj.org/article/cd52335b25a34f74af81b82a76dc43d9
Autor:
Masamitsu Okada, Yohei Misumi, Teruaki Masuda, Seiji Takashio, Masayoshi Tasaki, Hiroaki Matsushita, Akihiko Ueda, Yasuteru Inoue, Toshiya Nomura, Makoto Nakajima, Taro Yamashita, Satoru Shinriki, Hirotaka Matsui, Kenichi Tsujita, Yukio Ando, Mitsuharu Ueda
Publikováno v:
ESC Heart Failure, Vol 8, Iss 2, Pp 1178-1185 (2021)
Abstract Aims Hereditary transthyretin (ATTRv) amyloidosis is the most frequent and representative form of autosomal dominant hereditary systemic amyloidosis. Disease‐modifying treatments of the disease are more effective during the early stages, a
Externí odkaz:
https://doaj.org/article/c4a6da5a24bf49bea09b0785f465d6f0
Publikováno v:
Biology, Vol 12, Iss 2, p 320 (2023)
The MATP/tau protein is hyperphosphorylated in Alzheimer’s patients. Therefore, research into the regulation of tau protein phosphorylation is important for understanding Alzheimer’s disease. HASPIN is a serine/threonine kinase that is expressed
Externí odkaz:
https://doaj.org/article/94ba20f9ae994c44b2e3fba721281c4d
Autor:
Morie Gertz, David Adams, Yukio Ando, João Melo Beirão, Sabahat Bokhari, Teresa Coelho, Raymond L. Comenzo, Thibaud Damy, Sharmila Dorbala, Brian M. Drachman, Marianna Fontana, Julian D. Gillmore, Martha Grogan, Philip N. Hawkins, Isabelle Lousada, Arnt V. Kristen, Frederick L. Ruberg, Ole B. Suhr, Mathew S. Maurer, Jose Nativi-Nicolau, Candida Cristina Quarta, Claudio Rapezzi, Ronald Witteles, Giampaolo Merlini
Publikováno v:
BMC Family Practice, Vol 21, Iss 1, Pp 1-12 (2020)
Abstract Background Transthyretin amyloidosis (also known as ATTR amyloidosis) is a systemic, life-threatening disease characterized by transthyretin (TTR) fibril deposition in organs and tissue. A definitive diagnosis of ATTR amyloidosis is often a
Externí odkaz:
https://doaj.org/article/78acd23bfad24bcdb52811fe1e3f573a